Novel antioxidant peptides obtained by alcalase hydrolysis of Erythrina edulis (pajuro) protein

Arturo Intiquilla, Karim Lizeth Jimenez Aliaga, Fanny Guzmán, Claudio A. Alvarez, Amparo Iris Zavaleta Pesantes, Victor Luis Izaguirre Pasquel, Blanca Hernández-Ledesma

Research output: Contribution to journalArticlepeer-review

13 Scopus citations


BACKGROUND: Oxidative reactions are responsible for the changes in quality during food processing and storage. Oxidative stress is also involved in multiple chronic diseases, such as cardiovascular and neurodegenerative disorders, diabetes, cancer, and aging. The consumption of dietary antioxidants has been demonstrated to help to reduce the oxidative damage in both the human body and food systems. In this study, the potential of Erythrina edulis (pajuro) protein as source of antioxidant peptides was evaluated. RESULTS: Pajuro protein concentrate hydrolyzed by alcalase for 120 min showed potent ABTS ·+ and peroxyl radical scavenging activity with Trolox equivalent antioxidant capacity (TEAC) and oxygen radical absorbance capacity (ORAC) values of 1.37 ± 0.09 µmol TE mg −1 peptide and 2.83 ± 0.07 µmol TE mg −1 peptide, respectively. Fractionation of the hydrolyzate to small peptides resulted in increased antioxidant activity. De novo sequencing of most active fractions collected by chromatographic analysis enabled 30 novel peptides to be identified. Of these, ten were synthesized and their radical activity evaluated, demonstrating their relevant contribution to the antioxidant effects observed for pajuro protein hydrolyzate. CONCLUSIONS: The sequences identified represent an important advance in the molecular characterization of the pajuro protein, demonstrating its potential as a source of antioxidant peptides for food and nutraceutical applications.

Original languageEnglish
Pages (from-to)2420-2427
Number of pages8
JournalJournal of the Science of Food and Agriculture
Issue number5
StatePublished - 30 Mar 2019
Externally publishedYes

Bibliographical note

Funding Information:
This work has received financial support from projects 186-FINCyT-IA-2013 (Programa Nacional de Innovación para la Competividad y Productividad) (Innovate-Peru), N∘ 007-FONDECYT-2014 (Fondo Nacional de Desarrollo Científico, Tecnológico y de Innovación Tecnológica-Peru), and AGL2015-66886-R (Ministry of Economy and Competitiveness, MINECO, Spain).


  • alcalase hydrolysis
  • antioxidant activity
  • bioactive peptides
  • Erythrina edulis

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